Description
We are seeking an experienced Clinical Research Associate (CRA) with Ophthalmology expertise to join our team. You will utilise your skills, knowledge, and clinical judgement to provide high-quality care for participants in clinical trials and respond to emergency situations based on clinical research standards.
Responsibilities:
- Conduct routine monitoring and close-out of clinical sites, maintain study files, and liaise with vendors
- Ensure study staff have received proper materials and instructions to safely enter patients into the study
- Verify informed consent procedures and protocol requirements are adhered to according to regulatory requirements
- Ensure data integrity by reviewing Case Report Forms (CRFs) and source documents
- Complete Serious Adverse Event (SAE) reporting and follow-up
- Independently perform CRF review and query generation
- Assist with training new employees and coordinate clinical projects
Requirements:
- University or college degree, or certification in a related allied health profession
- 3+ years of Clinical Monitoring experience
- Ophthalmology experience
- 30-50% overnight travel
Work Environment:
- Fast-paced environment with changing priorities
- Teamwork and people skills essential
- Technology-based with electronic data collection
Physical Requirements:
- Ability to sit for extended periods and operate a vehicle safely
- Repetitive hand movement and ability to make fast, simple, repeated movements
- Occasional crouching, stooping, and lifting of 15-20 lbs
Salary: $118,000 - $142,000 per year